Proteins as binding targets of isothiocyanates in cancer prevention.
about
Cancer prevention with promising natural products: mechanisms of action and molecular targetsNaturally Occurring Isothiocyanates Exert Anticancer Effects by Inhibiting Deubiquitinating EnzymesCancer chemoprevention with dietary isothiocyanates mature for clinical translational researchMechanisms of Nrf2/Keap1-dependent phase II cytoprotective and detoxifying gene expression and potential cellular targets of chemopreventive isothiocyanatesIdentification of cancer chemopreventive isothiocyanates as direct inhibitors of the arylamine N-acetyltransferase-dependent acetylation and bioactivation of aromatic amine carcinogensMolecular Mechanisms Underlying Anti-Inflammatory Actions of 6-(Methylsulfinyl)hexyl Isothiocyanate Derived from Wasabi (Wasabia japonica)Beyond Warburg effect--dual metabolic nature of cancer cells.No evident dose-response relationship between cellular ROS level and its cytotoxicity--a paradoxical issue in ROS-based cancer therapy.A Click Chemistry Approach to Identify Protein Targets of Cancer Chemopreventive Phenethyl Isothiocyanate.Viability and stress protection of chronic lymphoid leukemia cells involves overactivation of mitochondrial phosphoSTAT3Ser727.Nuclear factor-kappaB sensitizes to benzyl isothiocyanate-induced antiproliferation in p53-deficient colorectal cancer cellsThe molecular basis that unifies the metabolism, cellular uptake and chemopreventive activities of dietary isothiocyanates.Protection of humans by plant glucosinolates: efficiency of conversion of glucosinolates to isothiocyanates by the gastrointestinal microfloraModulation of protein quality control systems by food phytochemicals.Exploring the effects of isothiocyanates on chemotherapeutic drugs.Monitoring Keap1-Nrf2 interactions in single live cells.Naturally occurring products in cancer therapy.Identification of deubiquitinase targets of isothiocyanates using SILAC-assisted quantitative mass spectrometry.Growth-inhibitory activity of natural and synthetic isothiocyanates against representative human microbial pathogens.Isothiocyanates suppress the invasion and metastasis of tumors by targeting FAK/MMP-9 activity.Characterization of the covalent binding of allyl isothiocyanate to β-lactoglobulin by fluorescence quenching, equilibrium measurement, and mass spectrometry.Sulforaphene suppresses growth of colon cancer-derived tumors via induction of glutathione depletion and microtubule depolymerization.Competition-based, quantitative chemical proteomics in breast cancer cells identifies new target profiles for sulforaphane.Design, Synthesis, and Evaluation of ω-(Isothiocyanato)alkylphosphinates and Phosphine Oxides as Antiproliferative Agents.Sulforaphane interaction with amyloid beta 1-40 peptide studied by electrospray ionization mass spectrometry.Physiological relevance of covalent protein modification by dietary isothiocyanates.KEAP1 and Done? Targeting the NRF2 Pathway with Sulforaphane.Sulforaphene enhances radiosensitivity of hepatocellular carcinoma through suppression of the NF-κB pathway.BAG3 Protein Is Involved in Endothelial Cell Response to Phenethyl Isothiocyanate.Discovering proteasomal deubiquitinating enzyme inhibitors for cancer therapy: lessons from rational design, nature and old drug repositionPlant Defensive β-Glucosidases Resist Digestion and Sustain Activity in the Gut of a Lepidopteran HerbivoreSulforaphane metabolites reduce resistance to paclitaxel via microtubule disruption
P2860
Q27006530-5F039A71-1094-4A72-BF25-D9E3B32849EEQ28269486-AD7B760B-7C27-4FEF-96C5-43D788DB074DQ28269727-C06A4581-B8E2-4940-BD4C-BC79787E2A09Q28384271-1B0D1465-80EE-447D-B317-2FE172D990A9Q28829316-60B63556-133C-4341-8D37-88B309A1F78DQ30394902-F309BA67-8A8B-43A5-8294-FB3CF3BC11ABQ33600827-31E09C87-F5C8-4FB9-A605-5E3888EAF586Q33647236-403F78A3-7005-42A5-B1C6-7390E934D1E1Q33907551-37457C5B-0ECD-4442-9649-2DC7DFCCC9EEQ34541525-44FE7275-C693-4365-8BA7-EF7F533E0C30Q34662321-9A1AA649-6ADA-4E2F-8778-D72E68299DE8Q35747310-DD280BFB-007D-4667-9EEC-4504402DB7ADQ36201654-26F2CD80-D211-4F6A-8420-55291ED0396EQ38109158-67C5CB58-7EBE-4C85-8AAA-C294FF55BA30Q38148572-3EFC829B-59F1-4219-B5C1-0A342C1F9E49Q38200391-C7DB9FA9-EAAF-4F43-90D6-2AE61B34AC92Q38504050-BF332443-34A1-4D84-A0C7-0F1EE0D3553EQ41612750-BBB2C5A9-81A0-4027-BEA1-593C544A1A9CQ42087068-33A96FF5-3494-46C4-81D3-978B2CA7D1E2Q42124894-014C8D5D-B893-48E7-826D-F16407C0E16AQ46092690-35C6CE66-FF3A-4816-BB80-76386FC9078DQ46589674-407B1919-8885-48F3-9F7E-6B4349CFD5E0Q48237312-FF5A6AA5-CA64-45DA-854B-937C70A941E4Q48240219-50787B8D-990F-4D8E-AC19-31A5256D2102Q48570518-AA855041-A893-4F79-9B08-149EE18AB45CQ49218143-FAB99C1B-8160-48DA-9ECD-2E709C10F4E3Q49834826-C932E439-6DBA-491C-AEB0-5E28804D0908Q51083903-C7ADFC1E-CE16-4D99-BAAC-51250360028FQ55411962-9BCFF1BF-5F4A-47A9-8EF2-C43F2CEC1BD4Q57163862-4731D7FE-693B-4640-B804-D7FF11963321Q57817624-B14FCA06-3128-48BF-A2F7-148AC0B59236Q59137604-4D634339-8BDB-42A7-A720-AF0D64F2A10E
P2860
Proteins as binding targets of isothiocyanates in cancer prevention.
description
2011 nî lūn-bûn
@nan
2011 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Proteins as binding targets of isothiocyanates in cancer prevention.
@ast
Proteins as binding targets of isothiocyanates in cancer prevention.
@en
type
label
Proteins as binding targets of isothiocyanates in cancer prevention.
@ast
Proteins as binding targets of isothiocyanates in cancer prevention.
@en
prefLabel
Proteins as binding targets of isothiocyanates in cancer prevention.
@ast
Proteins as binding targets of isothiocyanates in cancer prevention.
@en
P2093
P2860
P356
P1433
P1476
Proteins as binding targets of isothiocyanates in cancer prevention.
@en
P2093
Anthony J Di Pasqua
Fung-Lung Chung
P2860
P304
P356
10.1093/CARCIN/BGR111
P407
P577
2011-06-10T00:00:00Z